Canonical Allele Identifier: CA910796133

Gene: ROBO1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.79380661G>T , CM000665.2:g.79380661G>T	GRCh38
NC_000003.11:g.79429811G>T , CM000665.1:g.79429811G>T	GRCh37
NC_000003.10:g.79512501G>T	NCBI36
NG_011729.1:g.392249C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464233.6:c.88+209163C>A MANE Select	ENSP00000420321.1:n.88+209163C>A
ENST00000464233.5:c.88+209163C>A	ENSP00000420321.1:n.88+209163C>A
NM_002941.3:c.88+209163C>A	NP_002932.1:n.88+209163C>A
XM_011533976.1:c.88+209163C>A	XP_011532278.1:n.88+209163C>A
XM_011533977.1:c.88+209163C>A	XP_011532279.1:n.88+209163C>A
XM_011533978.1:c.88+209163C>A	XP_011532280.1:n.88+209163C>A
XM_011533979.1:c.88+209163C>A	XP_011532281.1:n.88+209163C>A
XM_011533980.1:c.88+209163C>A	XP_011532282.1:n.88+209163C>A
XM_011533977.2:c.88+209163C>A	XP_011532279.1:n.88+209163C>A
XM_017006982.1:c.88+209163C>A	XP_016862471.1:n.88+209163C>A
XM_017006984.1:c.88+209163C>A	XP_016862473.1:n.88+209163C>A
NM_002941.4:c.88+209163C>A MANE Select	NP_002932.1:n.88+209163C>A